FDA Adverse Event Malfunction Summary report: N

DISINFECTANT, MEDICAL DEVICES

MDR report key: 19596538 · Received June 21, 2024

Report

Report Number
MW5156508
Event Type
Malfunction
Date Received
June 21, 2024
Report Date
June 19, 2024
Manufacturer
SOCLEAN, INC.
Product Code
LRJ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TN, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND
Health Professional
*

Narratives

Description of Event or Problem · 0

THE OZONE SMELL IS TERRIBLE. MY HUSBAND IS KEEPING A TERRIBLE CHEST COUGH, THAT WILL NOT GO AWAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1183424 DISINFECTANT, MEDICAL DEVICES DISINFECTANT, MEDICAL DEVICES LRJ SOCLEAN, INC. SC1200

Patients

Seq Age Sex Outcome Treatment
1 Male